Anagram & Information om | Engelska ordet SNVS

Exempel på hur man kan använda SNVS i en mening

• Single nucleotide substitutions with an allele frequency of less than 1% are sometimes called single-nucleotide variants (SNVs).
• SNV calling from NGS data is any of a range of methods for identifying the existence of single nucleotide variants (SNVs) from the results of next generation sequencing (NGS) experiments.
• It is a type of variant annotation tool that compiles deleterious genetic variant prediction scores from programs such as PolyPhen, ClinVar, and CADD and annotates the SNVs, insertions, deletions, and CNVs of the provided genome.
• Somatic aneuploidy such as SNVs (single-nucleotide variations) and CNVs (copy number variations) have been particularly observed and linked to brain disfunctions when arising in prenatal brain development; anyway those somatic aneuploidy have been observed in rates of 1,3-40%, potentially increasing with age and for this reason they have been proposed as a mechanism to generate normal genetic diversity among neurons.

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